United States · FDA National Drug Code directory
BOTOX Cosmetic
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0023-3919_265710db-c7b9-42ff-9fc8-c24a936c1d87
- Product NDC
- 0023-3919
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- onabotulinumtoxinA
- Labeler
- Allergan, Inc.
- Marketing category
- BLA
- Marketing start / end (source format)
- 20080715
- Source listing expiry
- 20271231
Source-listed ingredients
- BOTULINUM TOXIN TYPE A — 50 [USP'U]/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, GLASS in 1 CARTON (0023-3919-50) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS · 0023-3919-50
- 1 VIAL, GLASS in 1 CARTON (0023-3919-51) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS · 0023-3919-51
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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